JP5719781B2 - 3−(1−{3−[5−(1−メチル−ピペリジン−4−イルメトキシ)−ピリミジン−2−イル]−ベンジル}−6−オキソ−1,6−ジヒドロ−ピリダジン−3−イル)−ベンゾニトリル塩酸塩の新規な多形体およびその製法 - Google Patents
3−(1−{3−[5−(1−メチル−ピペリジン−4−イルメトキシ)−ピリミジン−2−イル]−ベンジル}−6−オキソ−1,6−ジヒドロ−ピリダジン−3−イル)−ベンゾニトリル塩酸塩の新規な多形体およびその製法 Download PDFInfo
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- JP5719781B2 JP5719781B2 JP2011544793A JP2011544793A JP5719781B2 JP 5719781 B2 JP5719781 B2 JP 5719781B2 JP 2011544793 A JP2011544793 A JP 2011544793A JP 2011544793 A JP2011544793 A JP 2011544793A JP 5719781 B2 JP5719781 B2 JP 5719781B2
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- oxo
- dihydro
- methyl
- benzyl
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EP09000140 | 2009-01-08 | ||
EP09000140.5 | 2009-01-08 | ||
PCT/EP2009/008684 WO2010078897A1 (en) | 2009-01-08 | 2009-12-04 | Novel polymorphic forms of 3-(1-{3-[5-(1-methyl-piperidin-4ylmethoxy)-pyrimidin-2-yl]-benzyl}-6-oxo-1,6-dihydro-pyridazin-3-yl)-benzonitrile hydrochloride salt and processes of manufacturing thereof |
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JP2014231814A Active JP5860126B2 (ja) | 2009-01-08 | 2014-11-14 | 3−(1−{3−[5−(1−メチル−ピペリジン−4−イルメトキシ)−ピリミジン−2−イル]−ベンジル}−6−オキソ−1,6−ジヒドロ−ピリダジン−3−イル)−ベンゾニトリル塩酸塩の新規な多形体およびその製法 |
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Families Citing this family (17)
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US8710058B2 (en) * | 2009-01-08 | 2014-04-29 | Merck Patent Gmbh | Polymorphic forms of 3-(1-{3-[5-(1-methyl-piperidin-4-ylmethoxy)-pyrimidin-2-yl]-benzyl}-6-oxo-1,6-dihydro-pyridazin-3-yl)-benzonitrile hydrochloride salt and processes of manufacturing thereof |
US20150044211A1 (en) * | 2012-03-19 | 2015-02-12 | Merck Patent Gmbh | Combination of a 6-oxo-1,6-dihydro-pyridazine derivative having anti-cancer activity with other anti-tumor compounds |
PL2914264T3 (pl) * | 2012-11-02 | 2017-12-29 | Merck Patent Gmbh | Pochodna 6-okso-1,6-dihydropirydazyny do zastosowania w leczeniu raka wątrobowokomórkowego (hcc) |
CA2935889C (en) * | 2014-01-07 | 2022-08-16 | Merck Patent Gmbh | A 6-oxo-1,6-dihydro-pyridazine derivative for the use for the treatment of renal cell carcinoma (rcc) |
KR20170090499A (ko) | 2014-12-12 | 2017-08-07 | 메르크 파텐트 게엠베하 | Egfr 억제제와 항암 활성을 갖는 6-옥소-1,6-디히드로-피리다진 유도체의 조합 |
US11179392B2 (en) | 2015-04-03 | 2021-11-23 | Impact Therapeutics, Inc. | Solid pharmaceutical formulation of PARP inhibitors and use thereof |
WO2016192831A1 (en) | 2015-05-29 | 2016-12-08 | Merck Patent Gmbh | Compositions of anions and cations with pharmacological activity |
KR20180092096A (ko) | 2017-02-08 | 2018-08-17 | 에이비온 주식회사 | 트리아졸로 피라진 유도체의 신규한 다형체 및 이의 제조 방법 |
US11465986B2 (en) | 2018-04-26 | 2022-10-11 | Fujian Akeylink Biotechnology Co., Ltd. | Crystal form of c-MET inhibitor and salt form thereof and preparation method therefor |
PT3996688T (pt) * | 2019-07-10 | 2023-11-29 | Merck Patent Gmbh | Preparação farmacêutica |
WO2022063869A2 (en) | 2020-09-24 | 2022-03-31 | Merck Patent Gmbh | Compounds for the treatment of viral infections |
KR102489160B1 (ko) | 2021-05-26 | 2023-01-18 | 주식회사 이노큐어테라퓨틱스 | 피페리딘디온 유도체 |
WO2022250350A1 (ko) | 2021-05-26 | 2022-12-01 | 주식회사 이노큐어테라퓨틱스 | 피페리딘디온 유도체 |
EP4346829A1 (en) | 2021-06-04 | 2024-04-10 | Merck Patent GmbH | Compounds for the treatment of glioblastoma |
CN114394957B (zh) * | 2021-12-24 | 2023-05-09 | 武汉九州钰民医药科技有限公司 | Met抑制剂盐酸特泊替尼的制备方法 |
KR20230155324A (ko) | 2022-05-03 | 2023-11-10 | 주식회사 이노큐어테라퓨틱스 | 피페리딘디온 유도체 |
CN116768868B (zh) * | 2023-08-15 | 2023-12-08 | 云南省药物研究所 | 一种哒嗪酮硫代衍生物及其制备方法和应用 |
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US7094909B2 (en) * | 2001-06-11 | 2006-08-22 | Agouron Pharmaceuticals, Inc. | HIV protease inhibitors, compositions containing the same, their pharmaceutical uses and materials for their synthesis |
US7169932B2 (en) * | 2001-06-11 | 2007-01-30 | Pfizer Inc. | HIV protease inhibitors, compositions containing the same, their pharmaceutical uses, material for their synthesis |
CA2536135C (en) * | 2003-08-19 | 2012-05-22 | Boehringer Ingelheim International Gmbh | Multivitamin syrup for children or young adults |
WO2005026114A1 (en) * | 2003-09-17 | 2005-03-24 | Pfizer Inc. | Hiv protease inhibitors, compositions containing the same and their pharmaceutical uses |
TW200616634A (en) * | 2004-10-01 | 2006-06-01 | Bristol Myers Squibb Co | Crystalline forms and process for preparing spiro-hydantoin compounds |
WO2006043145A1 (en) * | 2004-10-21 | 2006-04-27 | Pfizer Inc. | Inhibitors of hepatitis c virus protease, and compositions and treatments using the same |
CN101052633A (zh) * | 2004-11-02 | 2007-10-10 | 辉瑞大药厂 | 制备吲唑化合物的方法 |
BRPI0518203A2 (pt) * | 2004-11-02 | 2009-03-10 | Pfizer | mÉtodos para preparaÇço de compostos indazol |
DE102005057924A1 (de) * | 2005-12-05 | 2007-06-06 | Merck Patent Gmbh | Pyridazinonderivate |
KR101402474B1 (ko) * | 2006-04-26 | 2014-06-19 | 제넨테크, 인크. | 포스포이노시티드 3-키나제 억제제 화합물 및 이를 포함하는 약학적 조성물 |
US7820812B2 (en) * | 2006-07-25 | 2010-10-26 | Abbott Laboratories | Methods of manufacturing crystalline forms of rapamycin analogs |
US7812032B2 (en) * | 2006-07-25 | 2010-10-12 | Abbott Laboratories | Crystalline forms of rapamycin analogs |
DE102007032507A1 (de) * | 2007-07-12 | 2009-04-02 | Merck Patent Gmbh | Pyridazinonderivate |
US8710058B2 (en) * | 2009-01-08 | 2014-04-29 | Merck Patent Gmbh | Polymorphic forms of 3-(1-{3-[5-(1-methyl-piperidin-4-ylmethoxy)-pyrimidin-2-yl]-benzyl}-6-oxo-1,6-dihydro-pyridazin-3-yl)-benzonitrile hydrochloride salt and processes of manufacturing thereof |
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